First Trimester Prenatal Treatment and Molecular Genetic Diagnosis of Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency)*-Reference-Cited by-同舟云学术

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First Trimester Prenatal Treatment and Molecular Genetic Diagnosis of Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency)*

Published:1990-04 Issue:4 Volume:70 Page:838-848
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

SPEISER PHYLLIS W.,LAFORGIA NICOLA,KATO KOJI,PAREIRA JUDITH,KHAN RAFIYA,YANG SOO YOUNG,WHORWOOD CHRISTOPHER,WHITE PERRIN C.,ELIAS SHERMAN,SCHRIOCK ELIZABETH,SCHRIOCK ELDON,SIMPSON JOE LEIGH,TASLIMI MARK,NAJJAR JENNIFER,MAY STEVEN,MILLS GARY,CRAWFORD CHRISTOPHER,NEW MARIA I.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/70/4/838/10508488/jcem0838.pdf

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1. The history of prenatal diagnosis of congenital adrenal hyperplasia;Genetic Steroid Disorders;2023

2. Contemporary prenatal genetic diagnosis for congenital adrenal hyperplasia: preimplantation genetic testing and maternal cell-free DNA;Genetic Steroid Disorders;2023

3. Pitfalls of prenatal and newborn screening in congenital adrenal hyperplasia: a narrative review;Pediatric Medicine;2022-01

4. Current perspective and scope of fetal therapy: part 2;The Journal of Maternal-Fetal & Neonatal Medicine;2020-11-01

5. Disorders of Sex Development;Yen and Jaffe's Reproductive Endocrinology;2019

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